- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00212927
Continuity of Care and Outcomes After Discharge From Hospital
August 31, 2015 updated by: Ottawa Hospital Research Institute
The Association of Provider Continuity and Information Continuity With Patient Outcomes After Discharge From Hospital
1. INTRODUCTION: Continuity of care (COC) occurs when separate elements of patient care are connected.
COC is made up primarily of Continuity of Provider (COP) and Continuity of Information (COI).
Many authorities believe that COC is essential to high-quality care.
Previous studies have shown poor COC in varied populations.
Many studies have shown that increased COC has been associated with improved intermediate outcomes.
However, no study has definitively determined whether COC or either of its components is associated with important outcomes.
The Ontario-Outcomes After the Hospitalization (Ontario-OAtH) study will enroll 5900 adults who are discharged to the community from medical and surgical services from 13 teaching and community hospitals in 5 regions across Ontario.
Patients will be followed for 6 months to record details about all interactions with the health care system.
This information will give us a detailed measure of both provider and information continuity for all patients over time.
The Ontario-OAtH study will have the power to precisely determine whether COC is associated with time to urgent readmission or death after hospital discharge.
Since COC is potentially modifiable, the Ontario-OAtH study will give us essential information required for designing interventions to improve outcomes for patients after they are discharged from hospital.
Study Overview
Status
Completed
Conditions
Detailed Description
See above
Study Type
Observational
Enrollment (Anticipated)
5900
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Ontario
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Ottawa, Ontario, Canada, K1Y 4E9
- Ottawa Health Research Institute
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- discharged to the community from medical and surgical services
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Carl Van Walraven, MD, OHRI
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2002
Study Completion (Actual)
December 1, 2006
Study Registration Dates
First Submitted
September 13, 2005
First Submitted That Met QC Criteria
September 13, 2005
First Posted (Estimate)
September 21, 2005
Study Record Updates
Last Update Posted (Estimate)
September 2, 2015
Last Update Submitted That Met QC Criteria
August 31, 2015
Last Verified
July 1, 2007
More Information
Terms related to this study
Other Study ID Numbers
- carl001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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